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Materials-Based Strategies for Multi-Enzyme Immobilization and Co-Localization: A Review

机译:基于材料的多酶固定化和共定位策略:综述

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摘要

Immobilized enzymes as biocatalysts have great potential both scientifically and industrially because of their technological and economic importance. Their highly efficient catalytic mechanisms and reusability have made them excellent candidates for green and sustainable applications. Previous studies have primarily focused on single enzyme immobilization. However, there are many situations where a single enzyme cannot completely catalyze reactions and multiple enzymes working together in a cascade are needed. It is very challenging to efficiently drive the multistep reaction toward the desired direction, which is especially true when reactive intermediates are present. Nature overcomes this limitation through the use of multi-enzyme complexes (MECs) to promote the overall catalytic efficiency, which has inspired researchers to synthesize artificial MECs to controllably enhance the production of the desired compounds in multi-step reaction cascades in vitro. The most common approaches to synthesize artificial MECs are to use genetic engineering techniques to create fusion proteins or to co-localize multiple enzymes on suitable carriers. This review focuses on the latter with a particular emphasis on materials-based approaches to enzyme co-localization, which builds on techniques developed for single enzyme immobilization. The attachment techniques used in single enzyme immobilization are also effective in multiple enzyme colocalization, which has a direct impact on the overall enzyme orientation and activity. For carrier-based strategies, the platforms developed for single enzyme immobilization are also appropriate for attaching and co-localizing multiple enzymes. However, the involvement of multiple components in co-localization brings many challenges. The properties of different enzymes makes co-localization complicated when selecting attachment techniques and platforms to preserve enzymatic activity, because the structure and function of each component enzyme needs to be taken into consideration to preserve the overall enzyme activity. In addition, the relative position of the multiple enzymes in a confined space plays a significant role in the interactions between different enzymes, which makes spatial control important for co-localization. This review focuses on the potential of materials-based approaches for multiple enzyme co-localization for the design of sustainable multi-enzyme biocatalysts. A critical analysis of the attachment techniques and carriers platforms that have been used in enzyme immobilization and multienzyme co-localization in vitro is provided. Biotechnol. Bioeng. 2014;111: 209–222.
机译:固定化酶作为生物催化剂,由于其技术和经济重要性,在科学和工业上均具有巨大潜力。它们的高效催化机制和可重复使用性使其成为绿色和可持续应用的极佳候选者。先前的研究主要集中在单一酶的固定化上。但是,在许多情况下,单个酶不能完全催化反应,并且需要多个酶以级联方式协同工作。有效地朝着期望的方向驱动多步反应是非常具有挑战性的,当存在反应性中间体时尤其如此。大自然通过使用多酶复合物(MEC)来提高总体催化效率来克服这一局限性,这激发了研究人员合成人工MEC,以可控地增强体外多步反应级联反应中所需化合物的生产。合成人工MEC的最常见方法是使用基因工程技术来创建融合蛋白或将多种酶共定位在合适的载体上。本文主要针对后者,特别强调基于材料的酶共定位方法,该方法基于为单一酶固定化开发的技术。在单一酶固定化中使用的连接技术在多种酶共定位中也有效,这直接影响了整个酶的方向和活性。对于基于载体的策略,开发用于单一酶固定化的平台也适用于附着和共定位多种酶。然而,多个组件参与共同定位带来了许多挑战。选择连接技术和平台以保留酶活性时,不同酶的特性会使共定位变得复杂,因为需要考虑每种组分酶的结构和功能以保持总体酶活性。此外,多种酶在有限空间中的相对位置在不同酶之间的相互作用中起着重要作用,这使得空间控制对于共定位很重要。这篇综述着重于基于材料的多酶共定位方法在设计可持续多酶生物催化剂方面的潜力。提供了对已在体外酶固定和多酶共定位中使用的连接技术和载体平台的关键分析。生物技术。生恩2014; 111:209–222。

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